LogoFresh Jobs Ahead
MSD
MSD
H1B vizasi homiysiBiotexnologiyaLogistikaSog‘liqni saqlash

MSD saraton, yuqumli kasalliklar, yurak-qon tomir va metabolik holatlar, shuningdek, profilaktik tibbiy yordam kabi muhim sog‘liq muammolariga qarshi dori vositalari va vaksinalarni ishlab chiqadigan global biofarmatsevtika kompaniyasidir. Amerika Qo‘shma Shtatlari, Kanada va Puerto-Rikoda Merck & Co., Inc. nomi bilan tanilgan MSD ilmiy tadqiqotlarni ishlab chiqish va tijoriy tajriba bilan birlashtirib, odamlar va hayvonlar uchun tibbiy yechimlarni taqdim etadi.

Kompaniya faoliyati Inson salomatligi, Hayvonlar salomatligi hamda Tadqiqot va ishlanmalar yo‘nalishlarini qamrab oladi. Bu ilmiy, klinik, tijoriy, operatsion va korporativ jamoalarda faoliyat yurituvchi mutaxassislar uchun imkoniyatlar yaratadi. Dunyoning turli hududlarida faoliyat olib boradigan MSDdagi martaba imkoniyatlari tadqiqot, hamkorlik, inklyuzivlik va global salomatlik sohasidagi mas’uliyatli taraqqiyotga e’tiborni aks ettiradi.

LinkedIn
Kompaniyadagi ish o‘rinlari

Executive Director, R&D Compliance, Global Medical and Scientific Affairs

Advise Merck’s global clinical development and medical affairs teams on pharmaceutical compliance. Oversee risk monitoring, policy implementation, senior counseling, and an international team of three.

USAmerika Qo‘shma ShtatlariNJNyu-JersiPAPensilvaniya
231 900 $ – 365 000 $ / yil
GibridTo‘liq stavkaYetakchiTalab Qilinadigan Til: inglizchaMuvofiqlik

Tavsif

  • Advise Global Clinical Development and Value & Implementation stakeholders worldwide on compliance matters.
  • Join the Value & Implementation Extended Leadership Team and serve as the compliance contact for its organizational leader.
  • Set strategic direction for oversight, data monitoring, analysis, and risk-based recommendations.
  • Brief senior management on compliance matters and external developments that affect internal compliance needs.
  • Advise Value & Implementation, Human Health stakeholders, and business operations on inherent risks.
  • Promote compliant business practices through policy development, compliance communications, and corrective actions.
  • Work with the research division on its Compliance Monitoring Plan to identify and address potential risks.
  • Support due diligence for later-stage business development and integration of completed acquisitions.
  • Coordinate with the Ethics & Compliance Office and International Legal and Compliance on headquarters-led and cross-regional practices.
  • Lead and develop a three-person team based in the United States and Europe.
  • Develop strong teams and talent across the compliance organization.

Talablar

  • Bachelor’s degree required.
  • At least 15 years of experience, with knowledge of laws, regulations, and policies governing pharmaceutical business practices, especially medical affairs.
  • Experience with advertising and promotion regulations, the Anti-Kickback Statute, and the Foreign Corrupt Practices Act.
  • Experience advising clients and influencing decision-makers, including senior leaders, on legal and compliance matters in life sciences.
  • Strong analytical ability to identify compliance risks and develop mitigation strategies.
  • Sound judgment, disciplined decision-making, emotional intelligence, and an effective advisory style.
  • Strong written and verbal communication and presentation skills.
  • Willingness to travel internationally as needed.
  • Ability to build collaborative relationships across functions, divisions, and regions.
  • Familiarity with research and human health organizations and their activities.
  • Experience developing or implementing written policies and guidance.
  • Experience leading and developing teams, or a strong interest in people management.
  • An advanced degree in science, business, or policy is preferred.
  • A JD from a US-accredited law school or an equivalent degree from outside the United States is strongly preferred.
  • Required skills include compliance program development, compliance reporting, cross-cultural awareness, attention to detail, ethical compliance, sound judgment, leadership, metrics analysis, people management, policy implementation, regulatory compliance audits, regulatory reporting, stakeholder management, technical documentation management, and training and development.

Imtiyozlar

  • Annual bonus and long-term incentive, where applicable.
  • Medical, dental, vision, and other insurance coverage for employees and their families.
  • Retirement benefits, including a 401(k).
  • Paid holidays.
  • Vacation leave.
  • Compassionate leave and sick days.
  • Hybrid work arrangement.

O‘xshash ish o‘rinlari

CVS Health

CVS Health Business Compliance Manager, Requests for Information

CVS Health
Chakana savdoSog‘liqni saqlashTibbiy sug‘urta
USAmerika Qo‘shma ShtatlariALAlabamaAZArizonaCTKonnektikutFLFloridaKSKanzasKYKentukkiLALuizianaNJNyu-JersiNCShimoliy KarolinaOHOgayoOKOklaxomaPAPensilvaniyaRIRod-AylendTNTennessiTXTexas
66 330 $ – 145 860 $ / yil
GibridTo‘liq stavkaSeniorYetakchiTalab Qilinadigan Til: inglizchaMuvofiqlik

Oversee regulatory information requests across CVS Health operations and jurisdictions. Lead analysts and coordinate compliant responses with Legal, Compliance, and Operations.

Ochish
Johnson & Johnson

Senior Regulatory Affairs Manager, Biomaterials

Johnson & Johnson
H1B vizasi homiysiBiotexnologiyaFarmatsevtika mahsulotlariSog‘liqni saqlash
USAmerika Qo‘shma ShtatlariMAMassachusetsPAPensilvaniya
117 000 $ – 201 250 $ / yil
GibridTo‘liq stavkaSeniorYetakchiTalab Qilinadigan Til: inglizchaMuvofiqlik

Lead regulatory strategy for Johnson & Johnson Orthopaedics’ biomaterials, biologics, and combination product programs. Oversee submissions, due diligence, and regulatory support for external innovation partnerships.

Ochish
Johnson & Johnson

Senior Manager, Regulatory Affairs – Biomaterials | Johnson & Johnson

Johnson & Johnson
H1B vizasi homiysiFarmatsevtika mahsulotlariSog‘liqni saqlashTibbiy sug‘urta
USAmerika Qo‘shma ShtatlariMAMassachusetsPAPensilvaniya
117 000 $ – 201 250 $ / yil
GibridTo‘liq stavkaSeniorYetakchiTalab Qilinadigan Til: inglizchaMuvofiqlik

Lead regulatory strategy for biomaterials, biologics, and combination products at Johnson & Johnson Orthopaedics. Guide submissions, external innovation reviews, and global approvals from development through product lifecycle management.

Ochish
RhyGaze

Regulyator operatsiyalari direktori | RhyGaze | Filadelfiyada gibrid ish

RhyGaze
BiotexnologiyaFarmatsevtika mahsulotlariSog‘liqni saqlash
USAmerika Qo‘shma ShtatlariPAPensilvaniyaGibridTo‘liq stavkaYetakchiTalab Qilinadigan Til: inglizchaMuvofiqlik
Google Cloud Platform

Gen terapiyasini ishlab chiqishda regulyator operatsiyalariga rahbarlik qiling, Veeva RIM jarayonlari va global ariza topshirish tizimlarini yarating. Ko‘rish qobiliyatidan ayrilgan bemorlar uchun ko‘rishni tiklashga mo‘ljallangan davolash usullarini ilgari surishga yordam bering.

Ochish